The novel TRPM4 c.448G>T variant is associated with familial conduction disorders, cardiomyopathy, and sudden cardiac death

Cardiol J. 2022;29(3):514-516. doi: 10.5603/CJ.a2021.0157. Epub 2021 Dec 13.
No abstract available

MeSH terms

  • Cardiomyopathies* / complications
  • Cardiomyopathies* / diagnosis
  • Cardiomyopathies* / genetics
  • Death, Sudden, Cardiac / etiology
  • Heart Rate
  • Humans
  • Pedigree
  • TRPM Cation Channels* / genetics

Substances

  • TRPM Cation Channels
  • TRPM4 protein, human